Issue 8, 2016

Copper(i) chloride promoted Csp2–N cross-coupling of 1,2-di(pyrimidin-2-yl) disulfides with amines: an efficient approach to obtain C2-amino functionalized pyrimidines

Abstract

The copper(I)-promoted cross-coupling of 1,2-di(pyrimidin-2-yl) disulfides with aromatic amines and aliphatic amines to deliver C–N coupling products in moderate to good yields is reported in this paper. Central to this strategy is the conversion of disulfides into aryl- and alkyl amines by a copper-promoted chemoselective C–S bond cleavage.

Graphical abstract: Copper(i) chloride promoted Csp2–N cross-coupling of 1,2-di(pyrimidin-2-yl) disulfides with amines: an efficient approach to obtain C2-amino functionalized pyrimidines

Supplementary files

Article information

Article type
Communication
Submitted
11 Dec 2015
Accepted
22 Jan 2016
First published
25 Jan 2016

Org. Biomol. Chem., 2016,14, 2395-2398

Copper(I) chloride promoted Csp2–N cross-coupling of 1,2-di(pyrimidin-2-yl) disulfides with amines: an efficient approach to obtain C2-amino functionalized pyrimidines

K. Wei, Z. Quan, Z. Zhang, Y. Da and X. Wang, Org. Biomol. Chem., 2016, 14, 2395 DOI: 10.1039/C5OB02535D

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